Canonical Allele Identifier: CA118164199
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1011814
gnomAD v2: 5-44335820-T-C
gnomAD v3: 5-44335718-T-C
gnomAD v4: 5-44335718-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44335718T>C , CM000667.2:g.44335718T>C GRCh38
NC_000005.9:g.44335820T>C , CM000667.1:g.44335820T>C GRCh37
NC_000005.8:g.44371577T>C NCBI36
NG_011446.1:g.57965A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.326-25188A>G MANE Select ENSP00000264664.4:n.326-25188A>G
ENST00000264664.4:c.326-25188A>G ENSP00000264664.4:n.326-25188A>G
NM_004465.1:c.326-25188A>G NP_004456.1:n.326-25188A>G
XM_005248264.2:c.326-25188A>G XP_005248321.1:n.326-25188A>G
XM_005248264.4:c.326-25188A>G XP_005248321.1:n.326-25188A>G
NM_004465.2:c.326-25188A>G MANE Select NP_004456.1:n.326-25188A>G